Open AccessDisturbed shear stress reduces Klf2 expression in arterial‐venous fistulae in vivo
Author(s) -
Yamamoto Kota,
Protack Clinton D.,
Kuwahara Go,
Tsuneki Masayuki,
Hashimoto Takuya,
Hall Michael R.,
Assi Roland,
Brownson Kirstyn E.,
Foster Trenton R.,
Bai Hualong,
Wang Mo,
Madri Joseph A.,
Dardik Alan
Publication year - 2015
Publication title -
physiological reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 39
ISSN - 2051-817X
DOI - 10.14814/phy2.12348
Subject(s) - klf2 , medicine , arteriovenous fistula , in vivo , fistula , inferior vena cava , aorta , pathology , endocrinology , anatomy , surgery , gene expression , biology , biochemistry , microbiology and biotechnology , gene
Abstract Laminar shear stress ( SS ) induces an antiproliferative and anti‐inflammatory endothelial phenotype and increases Klf2 expression. We altered the diameter of an arteriovenous fistula ( AVF ) in the mouse model to determine whether increased fistula diameter produces disturbed SS in vivo and if acutely increased disturbed SS results in decreased Klf2 expression. The mouse aortocaval fistula model was performed with 22, 25, or 28 gauge needles to puncture the aorta and the inferior vena cava. Duplex ultrasound was used to examine the AVF and its arterial inflow and venous outflow, and SS was calculated. Arterial samples were examined with western blot, immunohistochemistry, and immunofluorescence analysis for proteins and qPCR for RNA . Mice with larger diameter fistulae had diminished survival but increased AVF patency. Increased SS magnitudes and range of frequencies were directly proportional to the needle diameter in the arterial limb proximal to the fistula but not in the venous limb distal to the fistula, with 22‐gauge needles producing the most disturbed SS in vivo. Klf2 mRNA and protein expression was diminished in the artery proximal to the fistula in proportion to increasing SS . Increased fistula diameter produces increased SS magnitude and frequency, consistent with disturbed SS in vivo. Disturbed SS is associated with decreased mRNA and protein expression of Klf2. Disturbed SS and reduced Klf2 expression near the fistula are potential therapeutic targets to improve AVF maturation.